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T10269AHR antagonist 2AHR antagonist 2
AHR antagonist 2 is an antagonist of the aryl hydrocarbon receptor. The IC50s for human AHR and mouse AHR are 0.885 and 2.03 nM, respectively.
价 格：￥电议型 号：T10269产 地：中国大陆
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T7202ITEITE,Aryl Hydrocarbon Receptor,Inhibitor,inhibit,AhR
ITE is a potent endogenous agonist of aryl hydrocarbon receptor (AhR) (Ki : 3 nM), has immunosuppressive activity.
价 格：￥电议型 号：T7202产 地：中国大陆
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TN1451Brevifolincarboxylic acidGlucosidase,AhR,Brevifolincarboxylic acid,Inhibitor,Aryl Hydrocarbon Recept
Brevifolincarboxylic acid is a natural product isolated from Polygonum capitatum, it has inhibitory effect on the aryl hydrocarbon receptor (AhR). Brevifolincarboxylic acid is an α-glucosidase inhibitor with an IC50 of 323.46 μM.
价 格：￥电议型 号：TN1451产 地：中国大陆
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T39762AHR antagonist 5 free baseAHR antagonist 5 free base
AHR antagonist 5 free base is an orally active antagonist of AHR with IC50s of ~35-150 nM in human and rodent cell lines.
价 格：￥电议型 号：T39762产 地：中国大陆
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T6795CarbidopaCarbidopa,Aryl Hydrocarbon Receptor,peripheral,disease,AhR,cancer,Parkinson’s,pancreatic,In
Carbidopa is an aromatic-L-amino-acid decarboxylase inhibitor (IC50: 29±2 μM). It is used in PARKINSON DISEASE to reduce peripheral adverse effects of LEVODOPA.
价 格：￥电议型 号：T6795产 地：中国大陆
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TQ0257FICZinhibit,Inhibitor,Aryl Hydrocarbon Receptor,AhR,FICZ
FICZ is a potent aryl agonist for the hydrocarbon receptor (AhR, Kd: 70 pM).
价 格：￥电议型 号：TQ0257产 地：中国大陆
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T5622BAY-218AHR antagonist 1
AHR antagonist 1 is an aryl hydrocarbon receptor (AHR) antagonist , has an IC50 of 39.9 nM in human cell line.
价 格：￥电议型 号：T5622产 地：中国大陆
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T1610MetaxaloneMethaxalonum；Zorane；AHR438；Skelaxin；NSC170959；美他沙酮
Metaxalone (marketed by King Pharmaceuticals under the brand name Skelaxin ) is a muscle relaxant used to relax muscles and relieve pain caused by strains, sprains, and other musculoskeletal conditions.
价 格：￥电议型 号：T1610产 地：中国大陆
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T1409Methocarbamol美索巴莫；Lumirelax；AHR 85；Robaxin；Metocarbamol
Methocarbamol is a centrally acting muscle relaxant whose mode of action has not been established. It is used as an adjunct in the symptomatic treatment of musculoskeletal conditions associated with painful muscle spasm.
价 格：￥电议型 号：T1409产 地：中国大陆
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T1280Nepafenac奈帕芬胺；AHR 9434；AL 6515
Nepafenac is a Nonsteroidal Anti-inflammatory Drug. The mechanism of action of nepafenac is as a Cyclooxygenase Inhibitor. The chemical classification of nepafenac is Nonsteroidal Anti-inflammatory Compounds.
价 格：￥电议型 号：T1280产 地：中国大陆
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T12208Nepafenac D5Nepafenac D5,AHR-9434 D5,AL-6515 D5
Nepafenac D5 is the deuterium labeled Nepafenac, which is a selective inhibitor of COX-2 .
价 格：￥电议型 号：T12208产 地：美洲
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T1280NepafenacNepafenac,AL 6515,AHR 9434
Nepafenac is a Nonsteroidal Anti-inflammatory Drug. The mechanism of action of nepafenac is as a Cyclooxygenase Inhibitor. The chemical classification of nepafenac is Nonsteroidal Anti-inflammatory Compounds.
价 格：￥电议型 号：T1280产 地：美洲
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T1409MethocarbamolMethocarbamol,AHR 85,Robaxin
Methocarbamol is a centrally acting muscle relaxant whose mode of action has not been established. It is used as an adjunct in the symptomatic treatment of musculoskeletal conditions associated with painful muscle spasm.
价 格：￥电议型 号：T1409产 地：美洲
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T5622AHR antagonist 1AHR antagonist 1
AHR antagonist 1 is an aryl hydrocarbon receptor (AHR) antagonist , has an IC50 of 39.9 nM in human cell line.
价 格：￥电议型 号：T5622产 地：美洲
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T6424Bromfenac SodiumBromfenac Sodium,AHR 10282R,Bronuck
Bromfenac Sodium is a nonsteroidal anti-inflammatory drug (NSAID), which has anti-inflammatory activity and may block prostaglandin synthesis by inhibiting cyclooxygenase 1 and 2.
价 格：￥电议型 号：T6424产 地：美洲
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T80587Alunacedase alfa；化合物 Alunacedase alfaHrsACE2|||GSK 2586881；HrsACE2|||GSK 2586881
Alunacedase alfa (HrsACE2; GSK 2586881), a genetically modified human recombinant soluble angiotensin-converting enzyme-2 (hrsACE2), inhibits SARS-CoV-2 cell entry by competing with membrane-bound ACE2, offering potential in the research of SARS-CoV-2 [1] [2].
价 格：￥电议型 号：T80587产 地：中国大陆
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T79436AHR agonist 4；化合物 AHR agonist 4AHR agonist 4
AHR agonist 4 (compound 24e), as an Aryl hydrocarbon receptor (AHR) agonist, modulates the immune equilibrium between Th17/22 and Treg cells. It is a lead compound under investigation for anti-psoriasis drugs and demonstrates efficacy in mitigating imiquimod (IMQ)-induced psoriasis-like skin lesions [1].
价 格：￥电议型 号：T79436产 地：中国大陆
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T71590AHR-5645B fumarate；化合物 AHR-5645B fumarateAHR-5645B fumarate
AHR-5645B fumarate is a substituted benzamide that has been shown to inhibit 3H-spiperone binding to bovine anterior pituitary membranes.
价 格：￥电议型 号：T71590产 地：中国大陆
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T71053AHR-5333 mandelate；化合物 AHR-5333 mandelateAHR-5333 mandelate
AHR-5333 mandelate is an anti-allergy compound which has been shown to protect against antigen-induced anaphylactic collapse and ascaris antigen-induced skin hypersensitivity. AHR-5333 mandelate has also been shown to inhibit 5-HETE, LTB4 and LTC4 synthesis.
价 格：￥电议型 号：T71053产 地：中国大陆
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T69174AHR-5645B free base；化合物 AHR-5645B free baseAHR-5645B free base
AHR-5645B free base is a substituted benzamide which has been shown to inhibit 3H-spiperone binding to bovine anterior pituitary membranes.
价 格：￥电议型 号：T69174产 地：中国大陆
